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In order to further improve the bioavailability of BBR, the researchers encapsulated BBR in F127 micelles and designed an injectable ferrocene-cyclodextrin self-assembled oxidation-supramhydrogel drug delivery system to achieve high-quality diabetic wound healing (Liang et al., 2025)

There were three biological replicates for each of the blank and NAC groups

Its primary pharmacological characterization was published in European Journal of Endocrinology (PMID 9849822), where the authors identified it as the first growth-hormone-secretagogue receptor (GHSR-1a) agonist achieving GH-release selectivity comparable to GHRH in animal models

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